Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm2 |
A |
G |
3: 59,652,924 (GRCm39) |
K121R |
possibly damaging |
Het |
Abca13 |
G |
T |
11: 9,484,456 (GRCm39) |
W4342L |
probably damaging |
Het |
Abcg8 |
A |
T |
17: 84,995,958 (GRCm39) |
|
probably null |
Het |
Acaa1b |
A |
G |
9: 118,985,730 (GRCm39) |
L65P |
probably damaging |
Het |
Adam6a |
G |
T |
12: 113,509,556 (GRCm39) |
R643L |
probably benign |
Het |
Agbl2 |
A |
T |
2: 90,645,785 (GRCm39) |
R839S |
possibly damaging |
Het |
Ankrd17 |
T |
A |
5: 90,408,000 (GRCm39) |
N1406Y |
probably damaging |
Het |
Armh4 |
T |
C |
14: 50,005,932 (GRCm39) |
T588A |
probably damaging |
Het |
Bbx |
G |
T |
16: 50,086,608 (GRCm39) |
S96Y |
probably damaging |
Het |
Cdh12 |
T |
A |
15: 21,520,336 (GRCm39) |
|
probably null |
Het |
Cdh9 |
A |
C |
15: 16,823,361 (GRCm39) |
R114S |
probably benign |
Het |
Cenpo |
T |
G |
12: 4,266,683 (GRCm39) |
I142L |
probably benign |
Het |
Cfap69 |
T |
C |
5: 5,713,970 (GRCm39) |
K21E |
probably damaging |
Het |
Chmp4c |
A |
T |
3: 10,454,996 (GRCm39) |
D221V |
probably benign |
Het |
Cstf3 |
T |
A |
2: 104,486,101 (GRCm39) |
V447D |
possibly damaging |
Het |
Cwc22 |
A |
T |
2: 77,735,819 (GRCm39) |
C566S |
probably benign |
Het |
Dgkh |
A |
G |
14: 78,832,663 (GRCm39) |
M798T |
probably damaging |
Het |
Dnai2 |
T |
C |
11: 114,623,749 (GRCm39) |
V4A |
possibly damaging |
Het |
Dnai7 |
A |
C |
6: 145,121,926 (GRCm39) |
V631G |
probably benign |
Het |
Dnmbp |
T |
G |
19: 43,890,007 (GRCm39) |
I587L |
possibly damaging |
Het |
Dock6 |
A |
T |
9: 21,724,387 (GRCm39) |
M301K |
probably damaging |
Het |
Dock8 |
T |
C |
19: 25,038,521 (GRCm39) |
M69T |
probably benign |
Het |
Ears2 |
T |
C |
7: 121,643,801 (GRCm39) |
S386G |
probably benign |
Het |
Ecsit |
T |
C |
9: 21,983,817 (GRCm39) |
I371V |
probably benign |
Het |
Eif4a3 |
T |
C |
11: 119,184,737 (GRCm39) |
I216V |
probably benign |
Het |
Emp1 |
A |
G |
6: 135,357,128 (GRCm39) |
I69V |
probably damaging |
Het |
Epg5 |
A |
G |
18: 78,008,236 (GRCm39) |
D788G |
probably benign |
Het |
Eps15 |
A |
G |
4: 109,226,171 (GRCm39) |
K324E |
probably damaging |
Het |
Extl3 |
A |
G |
14: 65,315,071 (GRCm39) |
F37S |
probably benign |
Het |
Fam83g |
A |
G |
11: 61,585,994 (GRCm39) |
D194G |
probably damaging |
Het |
Gcc2 |
A |
G |
10: 58,112,485 (GRCm39) |
D1005G |
probably damaging |
Het |
Gm10226 |
T |
A |
17: 21,910,916 (GRCm39) |
H50Q |
possibly damaging |
Het |
Gm1110 |
A |
T |
9: 26,800,934 (GRCm39) |
V420E |
probably damaging |
Het |
Gm16503 |
A |
G |
4: 147,625,667 (GRCm39) |
R54G |
unknown |
Het |
Grin3b |
T |
C |
10: 79,810,432 (GRCm39) |
M646T |
probably damaging |
Het |
Grm8 |
T |
C |
6: 27,363,583 (GRCm39) |
D644G |
probably benign |
Het |
Gtf2i |
C |
A |
5: 134,275,702 (GRCm39) |
V660F |
probably damaging |
Het |
Heatr4 |
G |
T |
12: 84,002,591 (GRCm39) |
Q808K |
probably benign |
Het |
Hif3a |
T |
C |
7: 16,773,581 (GRCm39) |
S573G |
possibly damaging |
Het |
Htr2b |
C |
T |
1: 86,027,523 (GRCm39) |
V328M |
probably damaging |
Het |
Jph1 |
T |
C |
1: 17,162,279 (GRCm39) |
T128A |
probably damaging |
Het |
Kcnt1 |
T |
C |
2: 25,790,481 (GRCm39) |
V481A |
probably damaging |
Het |
Khk |
A |
G |
5: 31,087,962 (GRCm39) |
Y212C |
probably damaging |
Het |
Lgi2 |
T |
A |
5: 52,703,974 (GRCm39) |
Q219L |
probably benign |
Het |
Lipf |
T |
A |
19: 33,943,075 (GRCm39) |
Y128N |
probably benign |
Het |
Lipg |
A |
G |
18: 75,094,008 (GRCm39) |
V13A |
probably benign |
Het |
Lrrc8e |
T |
C |
8: 4,285,202 (GRCm39) |
S476P |
probably benign |
Het |
Map2k7 |
T |
G |
8: 4,295,795 (GRCm39) |
V425G |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,422,319 (GRCm39) |
S2451R |
probably damaging |
Het |
Mylk3 |
A |
G |
8: 86,053,821 (GRCm39) |
S629P |
probably damaging |
Het |
Nrp2 |
A |
T |
1: 62,801,906 (GRCm39) |
I450F |
probably damaging |
Het |
Or4c126 |
T |
C |
2: 89,824,148 (GRCm39) |
V137A |
probably benign |
Het |
Or8g50 |
A |
G |
9: 39,648,918 (GRCm39) |
D269G |
probably benign |
Het |
Osbpl11 |
T |
C |
16: 33,006,213 (GRCm39) |
S14P |
probably benign |
Het |
Osbpl11 |
T |
A |
16: 33,030,465 (GRCm39) |
V231D |
possibly damaging |
Het |
Parg |
T |
A |
14: 31,930,184 (GRCm39) |
|
probably benign |
Het |
Pax9 |
G |
T |
12: 56,743,923 (GRCm39) |
R190L |
possibly damaging |
Het |
Prss12 |
G |
A |
3: 123,300,144 (GRCm39) |
V752I |
probably benign |
Het |
Pstpip2 |
A |
G |
18: 77,922,892 (GRCm39) |
N34S |
probably damaging |
Het |
Rarg |
T |
C |
15: 102,160,880 (GRCm39) |
D53G |
probably benign |
Het |
Rbak |
T |
C |
5: 143,161,871 (GRCm39) |
K53R |
probably damaging |
Het |
Scgn |
A |
T |
13: 24,162,808 (GRCm39) |
S107R |
probably damaging |
Het |
Sema3c |
A |
G |
5: 17,932,399 (GRCm39) |
Q634R |
probably benign |
Het |
Serpinh1 |
A |
G |
7: 98,998,288 (GRCm39) |
L114P |
probably damaging |
Het |
Slc35f4 |
T |
C |
14: 49,541,380 (GRCm39) |
|
probably benign |
Het |
Sned1 |
A |
T |
1: 93,201,884 (GRCm39) |
I617F |
probably null |
Het |
Spata31 |
C |
T |
13: 65,070,359 (GRCm39) |
R836* |
probably null |
Het |
Spen |
A |
G |
4: 141,199,909 (GRCm39) |
L2883P |
probably damaging |
Het |
Stmn3 |
A |
T |
2: 180,949,073 (GRCm39) |
M140K |
possibly damaging |
Het |
Syn3 |
A |
G |
10: 86,190,208 (GRCm39) |
|
probably null |
Het |
Tamalin |
T |
C |
15: 101,124,850 (GRCm39) |
|
probably benign |
Het |
Tor4a |
A |
G |
2: 25,085,414 (GRCm39) |
V163A |
possibly damaging |
Het |
Ttc12 |
A |
G |
9: 49,371,698 (GRCm39) |
Y189H |
probably damaging |
Het |
Ubxn7 |
T |
G |
16: 32,200,577 (GRCm39) |
|
probably benign |
Het |
Unc5b |
G |
A |
10: 60,614,027 (GRCm39) |
T274I |
probably damaging |
Het |
Upk1b |
C |
A |
16: 38,596,548 (GRCm39) |
|
probably null |
Het |
Usp18 |
A |
G |
6: 121,245,513 (GRCm39) |
I296M |
probably benign |
Het |
Usp42 |
A |
G |
5: 143,700,811 (GRCm39) |
Y1071H |
probably damaging |
Het |
Vil1 |
A |
G |
1: 74,457,684 (GRCm39) |
T106A |
probably benign |
Het |
Vmn1r42 |
T |
A |
6: 89,821,949 (GRCm39) |
I207F |
probably benign |
Het |
Vmn1r63 |
A |
G |
7: 5,806,225 (GRCm39) |
F136L |
probably damaging |
Het |
Vopp1 |
C |
T |
6: 57,731,572 (GRCm39) |
V140I |
probably benign |
Het |
Wdhd1 |
T |
C |
14: 47,496,034 (GRCm39) |
D610G |
possibly damaging |
Het |
Wdr48 |
T |
A |
9: 119,741,483 (GRCm39) |
D142E |
probably benign |
Het |
Whrn |
A |
G |
4: 63,412,969 (GRCm39) |
Y10H |
probably damaging |
Het |
Zmat3 |
A |
G |
3: 32,397,497 (GRCm39) |
V216A |
probably benign |
Het |
Zmym2 |
C |
T |
14: 57,197,299 (GRCm39) |
R1356W |
probably damaging |
Het |
Zyg11b |
A |
T |
4: 108,129,480 (GRCm39) |
L44Q |
probably damaging |
Het |
|
Other mutations in Ambra1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00264:Ambra1
|
APN |
2 |
91,741,934 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00861:Ambra1
|
APN |
2 |
91,601,271 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL00911:Ambra1
|
APN |
2 |
91,598,027 (GRCm39) |
splice site |
probably benign |
|
IGL01371:Ambra1
|
APN |
2 |
91,655,631 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01532:Ambra1
|
APN |
2 |
91,715,977 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01620:Ambra1
|
APN |
2 |
91,741,757 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02147:Ambra1
|
APN |
2 |
91,598,064 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02170:Ambra1
|
APN |
2 |
91,597,432 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02173:Ambra1
|
APN |
2 |
91,748,013 (GRCm39) |
missense |
probably benign |
|
IGL02212:Ambra1
|
APN |
2 |
91,747,706 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02256:Ambra1
|
APN |
2 |
91,599,399 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02319:Ambra1
|
APN |
2 |
91,717,265 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02502:Ambra1
|
APN |
2 |
91,730,877 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02961:Ambra1
|
APN |
2 |
91,741,793 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0003:Ambra1
|
UTSW |
2 |
91,741,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R0098:Ambra1
|
UTSW |
2 |
91,598,056 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0173:Ambra1
|
UTSW |
2 |
91,640,564 (GRCm39) |
splice site |
probably benign |
|
R0414:Ambra1
|
UTSW |
2 |
91,706,084 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0579:Ambra1
|
UTSW |
2 |
91,654,810 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1212:Ambra1
|
UTSW |
2 |
91,599,381 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1241:Ambra1
|
UTSW |
2 |
91,601,241 (GRCm39) |
splice site |
probably benign |
|
R1467:Ambra1
|
UTSW |
2 |
91,716,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Ambra1
|
UTSW |
2 |
91,716,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R1533:Ambra1
|
UTSW |
2 |
91,717,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R2080:Ambra1
|
UTSW |
2 |
91,716,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R2083:Ambra1
|
UTSW |
2 |
91,596,945 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2112:Ambra1
|
UTSW |
2 |
91,706,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R2255:Ambra1
|
UTSW |
2 |
91,747,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R3407:Ambra1
|
UTSW |
2 |
91,740,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R3732:Ambra1
|
UTSW |
2 |
91,640,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R4111:Ambra1
|
UTSW |
2 |
91,730,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R4792:Ambra1
|
UTSW |
2 |
91,603,191 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4879:Ambra1
|
UTSW |
2 |
91,603,039 (GRCm39) |
intron |
probably benign |
|
R5007:Ambra1
|
UTSW |
2 |
91,602,655 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5261:Ambra1
|
UTSW |
2 |
91,715,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R6141:Ambra1
|
UTSW |
2 |
91,706,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R6364:Ambra1
|
UTSW |
2 |
91,603,661 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6413:Ambra1
|
UTSW |
2 |
91,599,429 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6868:Ambra1
|
UTSW |
2 |
91,747,878 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6888:Ambra1
|
UTSW |
2 |
91,599,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R6964:Ambra1
|
UTSW |
2 |
91,747,761 (GRCm39) |
nonsense |
probably null |
|
R6970:Ambra1
|
UTSW |
2 |
91,602,945 (GRCm39) |
intron |
probably benign |
|
R6982:Ambra1
|
UTSW |
2 |
91,747,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R7205:Ambra1
|
UTSW |
2 |
91,598,103 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7458:Ambra1
|
UTSW |
2 |
91,748,029 (GRCm39) |
missense |
probably benign |
0.26 |
R7786:Ambra1
|
UTSW |
2 |
91,598,141 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7812:Ambra1
|
UTSW |
2 |
91,596,911 (GRCm39) |
start codon destroyed |
probably benign |
0.00 |
R7825:Ambra1
|
UTSW |
2 |
91,598,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R7860:Ambra1
|
UTSW |
2 |
91,603,838 (GRCm39) |
missense |
probably benign |
0.27 |
R8190:Ambra1
|
UTSW |
2 |
91,602,697 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8779:Ambra1
|
UTSW |
2 |
91,747,719 (GRCm39) |
missense |
probably benign |
0.05 |
R9044:Ambra1
|
UTSW |
2 |
91,740,434 (GRCm39) |
intron |
probably benign |
|
R9062:Ambra1
|
UTSW |
2 |
91,740,662 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9707:Ambra1
|
UTSW |
2 |
91,640,476 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ambra1
|
UTSW |
2 |
91,730,953 (GRCm39) |
missense |
possibly damaging |
0.82 |
Z1177:Ambra1
|
UTSW |
2 |
91,706,131 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Ambra1
|
UTSW |
2 |
91,599,344 (GRCm39) |
missense |
possibly damaging |
0.81 |
|